http://www.cnr.it/ontology/cnr/individuo/prodotto/ID304135
Palladium-Catalyzed Cross-Coupling of Styrenes with Aryl Methyl Ketones in Ionic Liquids: Direct Access to Cyclopropanes (Articolo in rivista)
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- Label
- Palladium-Catalyzed Cross-Coupling of Styrenes with Aryl Methyl Ketones in Ionic Liquids: Direct Access to Cyclopropanes (Articolo in rivista) (literal)
- Anno
- 2014-01-01T00:00:00+01:00 (literal)
- Http://www.cnr.it/ontology/cnr/pubblicazioni.owl#doi
- 10.1002/anie.201408245 (literal)
- Alternative label
Cotugno, Pietro; Monopoli, Antonio; Ciminale, Francesco; Milella, Antonella; Nacci, Angelo (2014)
Palladium-Catalyzed Cross-Coupling of Styrenes with Aryl Methyl Ketones in Ionic Liquids: Direct Access to Cyclopropanes
in Angewandte Chemie (Int. ed., Print)
(literal)
- Http://www.cnr.it/ontology/cnr/pubblicazioni.owl#autori
- Cotugno, Pietro; Monopoli, Antonio; Ciminale, Francesco; Milella, Antonella; Nacci, Angelo (literal)
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- Http://www.cnr.it/ontology/cnr/pubblicazioni.owl#numeroFascicolo
- Note
- ISI Web of Science (WOS) (literal)
- Http://www.cnr.it/ontology/cnr/pubblicazioni.owl#affiliazioni
- University of Bari; ICCOM-Consiglio Nazionale delle Ricerche (CNR) (literal)
- Titolo
- Palladium-Catalyzed Cross-Coupling of Styrenes with Aryl Methyl Ketones in Ionic Liquids: Direct Access to Cyclopropanes (literal)
- Abstract
- The combined use of Pd(OAc)(2), Cu(OAc)(2), and dioxygen in molten tetrabutylammonium acetate (TBAA) promotes an unusual cyclopropanation reaction between aryl methyl ketones and styrenes. The process is a dehydrogenative cyclizing coupling that involves a twofold C H activation at the a-position of the ketone. The substrate scope highlights the flexibility of the catalyst; a reaction mechanism is also proposed. (literal)
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